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Compound Detail

CHEMBL502560

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N#Cc1ccc2cc1Oc1cccc(c1)CN1CC[C@@H](NCc3cncn3C2)C1=O

Basic Information

ChEMBL ID CHEMBL502560
Phase Preclinical
Structure Type MOL
InChI Key PCMOPVSFMUOUFR-OAQYLSRUSA-N
4
Targets
7
Activities
2
Assay Types
3
PK Parameters
6
Publications
0
Known Names

Molecular Properties

399.4
MW (Da)
2.80
ALogP
6
HBA
1
HBD
83.2
PSA (Ų)
0.63
QED
0
Ro5 Violations
0
Rot. Bonds

Drug Information

Molecule Type Small molecule
Availability Unknown
Chirality Unknown

Flags

First in Class Prodrug

Extended Properties

Molecular Formula C23H21N5O2
MW 399.45
Aromatic Rings 3
Heavy Atoms 30
NP-Likeness 0.40

Activity Summary

IC50 5 meas. best 9.18
EC50 2 meas. best 8.21

Target Activity Profile

Target Type Best pChEMBL Mean pChEMBL Best (nM) # Data
Protein farnesyltransferase
CHEMBL2095197
IC50 9.18 9.18 0.7 1
Protein farnesyltransferase
CHEMBL2094108
IC50 8.7 8.58 2.0 2
Protein farnesyltransferase
CHEMBL2094108
EC50 8.21 8.05 6.1 2
Voltage-gated inwardly rectifying potassium channel KCNH2
CHEMBL240
IC50 5.33 5.33 4700.0 1
Cytochrome P450 3A4
CHEMBL340
IC50 5.05 5.05 8900.0 1

Pharmacokinetic Data

Parameter Value Units Species
CL 9.0 mL.min-1.kg-1 Canis lupus familiaris
F 47.0 % Canis lupus familiaris
T1/2 0.78 hr Canis lupus familiaris

Activity Data Samples

Top measurements by pChEMBL value

Literature References

PubMed DOI Target Context # Activities
12036349 10.1021/jm010531d Protein farnesyltransferase 5
12036349 10.1021/jm010531d Canis familiaris 4
12036349 10.1021/jm010531d Cytochrome P450 3A4 2
12036349 10.1021/jm010531d Geranylgeranyl transferase type I 1
12036349 10.1021/jm010531d Voltage-gated inwardly rectifying potassium channel KCNH2 1
19534531 10.1021/jm900002x Voltage-gated inwardly rectifying potassium channel KCNH2 1

Data from ChEMBL 36 via Core Engine